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(3S,5R,6S,7E)-5,6-EPOXY-3-HYDROXY-7-MEGASTIGMEN-9-ONE

Compound with spectra: 3 NMR

(3S,5R,6S,7E)-5,6-EPOXY-3-HYDROXY-7-MEGASTIGMEN-9-ONE
SpectraBase Compound ID 6FsbpQEi7Kr
InChI InChI=1S/C13H20O3/c1-9(14)5-6-13-11(2,3)7-10(15)8-12(13,4)16-13/h5-6,10,15H,7-8H2,1-4H3/b6-5+/t10-,12+,13-/m0/s1
InChIKey VYKLRWGPNUVKNC-IRIVYCKASA-N
Mol Weight 224.3 g/mol
Molecular Formula C13H20O3
Exact Mass 224.141245 g/mol
Enantiomer InChIKey VYKLRWGPNUVKNC-ZMGSTWARSA-N

View Spectrum of (3S,5R,6S,7E)-5,6-EPOXY-3-HYDROXY-7-MEGASTIGMEN-9-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (3S,5R,6S,7E)-5,6-EPOXY-3-HYDROXY-7-MEGASTIGMEN-9-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.

View Spectrum of (3S,5R,6S,7E)-5,6-EPOXY-3-HYDROXY-7-MEGASTIGMEN-9-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (3-S,5-R,6-S,7-E)-5,6-EPOXY-3-HYDROXY-7-MEGASTIGMENE-9-ONE
  • 3-BETA-HYDROXY-5-ALPHA,6-ALPHA-EPOXY-7-MEGASTIGMEN-9-ONE
ANNUIONONE-D
3-Buten-2-one, 4-(4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]hept-1-yl)-
(3-R,5-R,6-S,7-E)-MEGASTIGMAN-7-EN-5,6-EPOXY-3-OL-9-ONE
(3S,5R,6S,7E,9R)-5,6-EPOXY-3,9-DIHYDROXY-7-MEGASTIGMENE
7-Oxabicyclo[4.1.0]heptan-3-ol, 6-(3-hydroxy-1-butenyl)-1,5,5-trimethyl-
(3-R,5-R,6-S,7-E,9-S)-MEGASTIGMAN-7-EN-5,6-EPOXY-3,9-DIOL
UIQSLOCCENWDIG-VTUFKNJISA-N
7-Oxabicyclo[4.1.0]heptan-3-ol, 6-(5-hydroxy-3-methyl-1,3-pentadienyl)-1,5,5-trimethyl-, [1R-[1.alpha.,3.beta.,6.alpha.(1E,3E)]]-
7-Oxabicyclo[4.1.0]heptan-3-ol, 6-(5-hydroxy-3-methyl-1,3-pentadienyl)-1,5,5-trimethyl-, [1R-[1.alpha.,3.alpha.,6.alpha.(1E,3E)]]-
[5,5-Dimethyl-6-(3-methyl-buta-1,3-dienyl)-7-oxa-bicyclo[4.1.0]hept-1-yl]-methanol
(3-S,5-R,6-R,7-E,9-R)-5,6,9-TRIHYDROXY-3-ISOPROPYLOXY-7-MEGASTIGMANE
Title Journal or Book Year
Chemical-constituent diversity of Tridax procumbens Canadian Journal of Chemistry 2008
Structure elucidation and phytotoxicity of C13 nor-isoprenoids from Cestrum parqui Phytochemistry 2004

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(3-R,5-R,6-S,7-E)-MEGASTIGMAN-7-EN-5,6-EPOXY-3-OL-9-ONE
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